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Cerebral salt-wasting syndrome due to hemorrhagic brain infarction: a case report

INTRODUCTION: Cerebral salt-wasting syndrome is a condition featuring hyponatremia and dehydration caused by head injury, operation on the brain, subarachnoid hemorrhage, brain tumor and so on. However, there are a few reports of cerebral salt-wasting syndrome caused by cerebral infarction. We descr...

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Autores principales: Tanaka, Tomotaka, Uno, Hisakazu, Miyashita, Kotaro, Nagatsuka, Kazuyuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4124770/
https://www.ncbi.nlm.nih.gov/pubmed/25055823
http://dx.doi.org/10.1186/1752-1947-8-259
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author Tanaka, Tomotaka
Uno, Hisakazu
Miyashita, Kotaro
Nagatsuka, Kazuyuki
author_facet Tanaka, Tomotaka
Uno, Hisakazu
Miyashita, Kotaro
Nagatsuka, Kazuyuki
author_sort Tanaka, Tomotaka
collection PubMed
description INTRODUCTION: Cerebral salt-wasting syndrome is a condition featuring hyponatremia and dehydration caused by head injury, operation on the brain, subarachnoid hemorrhage, brain tumor and so on. However, there are a few reports of cerebral salt-wasting syndrome caused by cerebral infarction. We describe a patient with cerebral infarction who developed cerebral salt-wasting syndrome in the course of hemorrhagic transformation. CASE PRESENTATION: A 79-year-old Japanese woman with hypertension and arrhythmia was admitted to our hospital for mild consciousness disturbance, conjugate deviation to right, left unilateral spatial neglect and left hemiparesis. Magnetic resonance imaging revealed a broad ischemic change in right middle cerebral arterial territory. She was diagnosed as cardiogenic cerebral embolism because atrial fibrillation was detected on electrocardiogram on admission. She showed hyponatremia accompanied by polyuria complicated at the same time with the development of hemorrhagic transformation on day 14 after admission. Based on her hypovolemic hyponatremia, she was evaluated as not having syndrome of inappropriate secretion of antidiuretic hormone but cerebral salt-wasting syndrome. She fortunately recovered with proper fluid replacement and electrolyte management. CONCLUSIONS: This is a rare case of cerebral infarction and cerebral salt-wasting syndrome in the course of hemorrhagic transformation. It may be difficult to distinguish cerebral salt-wasting syndrome from syndrome of inappropriate antidiuretic hormone, however, an accurate assessment is needed to reveal the diagnosis of cerebral salt-wasting syndrome because the recommended fluid management is opposite in the two conditions.
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spelling pubmed-41247702014-08-08 Cerebral salt-wasting syndrome due to hemorrhagic brain infarction: a case report Tanaka, Tomotaka Uno, Hisakazu Miyashita, Kotaro Nagatsuka, Kazuyuki J Med Case Rep Case Report INTRODUCTION: Cerebral salt-wasting syndrome is a condition featuring hyponatremia and dehydration caused by head injury, operation on the brain, subarachnoid hemorrhage, brain tumor and so on. However, there are a few reports of cerebral salt-wasting syndrome caused by cerebral infarction. We describe a patient with cerebral infarction who developed cerebral salt-wasting syndrome in the course of hemorrhagic transformation. CASE PRESENTATION: A 79-year-old Japanese woman with hypertension and arrhythmia was admitted to our hospital for mild consciousness disturbance, conjugate deviation to right, left unilateral spatial neglect and left hemiparesis. Magnetic resonance imaging revealed a broad ischemic change in right middle cerebral arterial territory. She was diagnosed as cardiogenic cerebral embolism because atrial fibrillation was detected on electrocardiogram on admission. She showed hyponatremia accompanied by polyuria complicated at the same time with the development of hemorrhagic transformation on day 14 after admission. Based on her hypovolemic hyponatremia, she was evaluated as not having syndrome of inappropriate secretion of antidiuretic hormone but cerebral salt-wasting syndrome. She fortunately recovered with proper fluid replacement and electrolyte management. CONCLUSIONS: This is a rare case of cerebral infarction and cerebral salt-wasting syndrome in the course of hemorrhagic transformation. It may be difficult to distinguish cerebral salt-wasting syndrome from syndrome of inappropriate antidiuretic hormone, however, an accurate assessment is needed to reveal the diagnosis of cerebral salt-wasting syndrome because the recommended fluid management is opposite in the two conditions. BioMed Central 2014-07-23 /pmc/articles/PMC4124770/ /pubmed/25055823 http://dx.doi.org/10.1186/1752-1947-8-259 Text en Copyright © 2014 Tanaka et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Case Report
Tanaka, Tomotaka
Uno, Hisakazu
Miyashita, Kotaro
Nagatsuka, Kazuyuki
Cerebral salt-wasting syndrome due to hemorrhagic brain infarction: a case report
title Cerebral salt-wasting syndrome due to hemorrhagic brain infarction: a case report
title_full Cerebral salt-wasting syndrome due to hemorrhagic brain infarction: a case report
title_fullStr Cerebral salt-wasting syndrome due to hemorrhagic brain infarction: a case report
title_full_unstemmed Cerebral salt-wasting syndrome due to hemorrhagic brain infarction: a case report
title_short Cerebral salt-wasting syndrome due to hemorrhagic brain infarction: a case report
title_sort cerebral salt-wasting syndrome due to hemorrhagic brain infarction: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4124770/
https://www.ncbi.nlm.nih.gov/pubmed/25055823
http://dx.doi.org/10.1186/1752-1947-8-259
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